The chemokine CXCL3 is responsible for the constitutive chemotactic activity of bovine milk for neutrophils

Molecular Immunology

Volumn 45, Issue 15, 2008, Pages 4020-4027

  Rainard, Pascal ^a   Riollet, Céline ^a   Berthon, Patricia ^a   Cunha, Patricia ^a   Fromageau, Angélina ^a   Rossignol, Christelle ^a   Gilbert, Florence B ^a  

^a UR1282   (France)

Author keywords

Cattle; Chemokine; CXCL1; CXCL2; CXCL3; Epithelium; Mammary gland; Milk

Indexed keywords

CHEMOKINE; CHEMOKINE CXCL3; CHEMOTAXIN; CXCL1 CHEMOKINE; INTERLEUKIN 8; MELANOMA GROWTH STIMULATORY ACTIVITY FACTOR; MESSENGER RNA; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; BREAST EPITHELIUM; CHEMOTAXIS; COW; IMMUNOHISTOCHEMISTRY; INFLAMMATION; LACTATION; MASS SPECTROMETRY; MILK; NEUTROPHIL; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

ANIMALS; CATTLE; CHEMOKINES, CXC; CHEMOTAXIS; ENZYME-LINKED IMMUNOSORBENT ASSAY; FEMALE; IMMUNOHISTOCHEMISTRY; MAMMARY GLANDS, ANIMAL; MILK; NEUTROPHILS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;

BOS; BOVINAE;

EID: 49649087382     PISSN: 01615890     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molimm.2008.06.010     Document Type: Article

References (42)

1. Addison C.L., Daniel T.O., Burdick M.D., Liu H., Ehlert J.E., Xue Y.Y., Buechi L., Walz A., Richmond A., and Strieter R.M. The CXC chemokine receptor 2, CXCR2, is the putative receptor for ELR + CXC chemokine-induced angiogenic activity. J. Immunol. 165 (2000) 5269-5277
2. Bacon K., Baggiolini M., Broxmeyer H., Horuk R., Lindley I., Mantovani A., Maysushima K., Murphy P., Nomiyama H., Oppenheim J., Rot A., Schall T., Tsang M., Thorpe R., Van Damme J., Wadhwa M., Yoshie O., Zlotnik A., and Zoon K. Chemokine/chemokine receptor nomenclature. J. Interferon Cytokine Res. 22 (2002) 1067-1068
3. Bannerman D.D., Paape M.J., Lee J.W., Zhao X., Hope J.C., and Rainard P. Escherichia coli and Staphylococcus aureus elicit differential innate immune responses following intramammary infection. Clin. Diagn. Lab. Immunol. 11 (2004) 463-472
4. Barber M.R., and Yang T.J. Chemotactic activities in nonmastitic and mastitic mammary secretions: presence of interleukin-8 in mastitic but not nonmastitic secretions. Clin. Diagn. Lab. Immunol. 5 (1998) 82-86
5. Barrio M.B., Rainard P., and Prevost G. LukM/LukF′-PV is the most active Staphylococcus aureus leukotoxin on bovine neutrophils. Microbes Infect. 8 (2006) 2068-2074
6. Bottcher M.F., Jenmalm M.C., Bjorksten B., and Garofalo R.P. Chemoattractant factors in breast milk from allergic and nonallergic mothers. Pediatr. Res. 47 (2000) 592-597
7. Burton J.L., and Erskine R.J. Immunity and mastitis. Some new ideas for an old disease. Vet. Clin. N. Am. Food Anim. Pract. 19 (2003) 1-45
8. Caswell J.L., Middleton D.M., and Gordon J.R. Production and functional characterization of recombinant bovine interleukin-8 as a specific neutrophil activator and chemoattractant. Vet. Immunol. Immunopathol. 67 (1999) 327-340
9. Craven N. Chemotactic factors for bovine neutrophils in relation to mastitis. Comp. Immunol. Microbiol. Infect. Dis. 9 (1986) 29-36
10. Gouwy M., Struyf S., Proost P., and Van Damme J. Synergy in cytokine and chemokine networks amplifies the inflammatory response. Cytokine Growth Factor Rev. 16 (2005) 561-580
11. Haston W.S., and Shields J.M. Neutrophil leucocyte chemotaxis: a simplified assay for measuring polarizing responses to chemotactic factors. J. Immunol. Methods 81 (1985) 229-237
12. Heaton M.P., Laegreid W.W., Beattie C.W., Smith T.P., and Kappes S.M. Identification and genetic mapping of bovine chemokine genes expressed in epithelial cells. Mamm. Genome 10 (1999) 128-133
13. Johnson II M.C., Kajikawa O., Goodman R.B., Wong V.A., Mongovin S.M., Wong W.B., Fox-Dewhurst R., and Martin T.R. Molecular expression of the alpha-chemokine rabbit GRO in Escherichia coli and characterization of its production by lung cells in vitro and in vivo. J. Biol. Chem. 271 (1996) 10853-10858
14. Lahouassa H., Moussay E., Rainard P., and Riollet C. Differential cytokine and chemokine responses of bovine mammary epithelial cells to Staphylococcus aureus and Escherichia coli. Cytokine 38 (2007) 12-21
15. Lahouassa H., Rainard P., Caraty A., and Riollet C. Identification and characterization of a new interleukin-8 receptor in bovine species. Mol. Immunol. 45 (2008) 1153-1164
16. Lee J., Horuk R., Rice G.C., Bennett G.L., Camerato T., and Wood W.I. Characterization of two high affinity human interleukin-8 receptors. J. Biol. Chem. 267 (1992) 16283-16287
17. Li F., and Gordon J.R. Il-8((3-73))K11R is a high affinity agonist of the neutrophil CXCR1 and CXCR2. Biochem. Biophys. Res. Commun. 286 (2001) 595-600
18. Li F., Zhang X., and Gordon J.R. CXCL8((3-73))K11R/G31P antagonizes ligand binding to the neutrophil CXCR1 and CXCR2 receptors and cellular responses to CXCL8/IL-8. Biochem. Biophys. Res. Commun. 293 (2002) 939-944
19. Maheshwari A., Christensen R.D., and Calhoun D.A. ELR + CXC chemokines in human milk. Cytokine 24 (2003) 91-102
20. Maheshwari A., Lu W., Lacson A., Barleycorn A.A., Nolan S., Christensen R.D., and Calhoun D.A. Effects of interleukin-8 on the developing human intestine. Cytokine 20 (2002) 256-267
21. Manlongat N., Yang T.J., Hinckley L.S., Bendel R.B., and Krider H.M. Physiologic-chemoattractant-induced migration of polymorphonuclear leukocytes in milk. Clin. Diagn. Lab. Immunol. 5 (1998) 375-381
22. Michie C.A., Tantscher E., Schall T., and Rot A. Physiological secretion of chemokines in human breast milk. Eur. Cytokine Netw. 9 (1998) 123-129
23. Miller M.D., and Krangel M.S. Biology and biochemistry of the chemokines: a family of chemotactic and inflammatory cytokines. Crit. Rev. Immunol. 12 (1992) 17-46
24. Mrsny R.J., Gewirtz A.T., Siccardi D., Savidge T., Hurley B.P., Madara J.L., and McCormick B.A. Identification of hepoxilin A3 in inflammatory events: a required role in neutrophil migration across intestinal epithelia. Proc. Natl. Acad. Sci. U.S.A. 101 (2004) 7421-7426
25. Mukaida N. Pathophysiological roles of interleukin-8/CXCL8 in pulmonary diseases. Am. J. Physiol. Lung Cell Mol. Physiol. 284 (2003) L566-L577
26. Murphy P.M., Baggiolini M., Charo I.F., Hebert C.A., Horuk R., Matsushima K., Miller L.H., Oppenheim J.J., and Power C.A. International union of pharmacology. XXII. Nomenclature for chemokine receptors. Pharmacol. Rev. 52 (2000) 145-176
27. Nathan C. Neutrophils and immunity: challenges and opportunities. Nat. Rev. Immunol. 6 (2006) 173-182
28. Nguyen D.A., and Neville M.C. Tight junction regulation in the mammary gland. J. Mammary Gland Biol. Neoplasia 3 (1998) 233-246
29. Paape M., Mehrzad J., Zhao X., Detilleux J., and Burvenich C. Defense of the bovine mammary gland by polymorphonuclear neutrophil leukocytes. J. Mammary Gland Biol. Neoplasia 7 (2002) 109-121
30. Persson K., Colditz I.G., Flapper P., Franklin N.A., and Seow H.F. Cytokine-induced inflammation in the ovine teat and udder. Vet. Immunol. Immunopathol. 53 (1996) 73-85
31. Rainard P. Effect of milk or colostrum on phagocytosis of glass- or plastic-adherent Streptococcus agalactiae by bovine granulocytes. Vet. Immunol. Immunopathol. 26 (1990) 203-208
32. Rainard P., and Riollet C. Innate immunity of the bovine mammary gland. Vet. Res. 37 (2006) 369-400
33. Rainard P., Sarradin P., Paape M.J., and Poutrel B. Quantification of C5a/C5a(desArg) in bovine plasma, serum and milk. Vet. Res. 29 (1998) 73-88
34. Riollet C., Mutuel D., Duonor-Cerutti M., and Rainard P. Determination and characterization of bovine interleukin-17 cDNA. J. Interferon Cytokine Res. 26 (2006) 141-149
35. Riollet C., Rainard P., and Poutrel B. Differential induction of complement fragment C5a and inflammatory cytokines during intramammary infections with Escherichia coli and Staphylococcus aureus. Clin. Diagn. Lab. Immunol. 7 (2000) 161-167
36. Seegers H., Fourichon C., and Beaudeau F. Production effects related to mastitis and mastitis economics in dairy cattle herds. Vet. Res. 34 (2003) 475-491
37. Shuster D.E., Kehrli Jr. M.E., Rainard P., and Paape M. Complement fragment C5a and inflammatory cytokines in neutrophil recruitment during intramammary infection with Escherichia coli. Infect. Immun. 65 (1997) 3286-3292
38. Srivastava M.D., Srivastava A., Brouhard B., Saneto R., Groh-Wargo S., and Kubit J. Cytokines in human milk. Res. Commun. Mol. Pathol. Pharmacol. 93 (1996) 263-287
39. Strieter R.M., Polverini P.J., Kunkel S.L., Arenberg D.A., Burdick M.D., Kasper J., Dzuiba J., Van Damme J., Walz A., Marriott D., et al. The functional role of the ELR motif in CXC chemokine-mediated angiogenesis. J. Biol. Chem. 270 (1995) 27348-27357
40. Struyf S., Gouwy M., Dillen C., Proost P., Opdenakker G., and Van Damme J. Chemokines synergize in the recruitment of circulating neutrophils into inflamed tissue. Eur. J. Immunol. 35 (2005) 1583-1591
41. Tsang V.C., and Wilkins P.P. Optimum dissociating condition for immunoaffinity and preferential isolation of antibodies with high specific activity. J. Immunol. Methods 138 (1991) 291-299
42. Wuyts A., Govaerts C., Struyf S., Lenaerts J.P., Put W., Conings R., Proost P., and Van Damme J. Isolation of the CXC chemokines ENA-78, GRO alpha and GRO gamma from tumor cells and leukocytes reveals NH2-terminal heterogeneity. Functional comparison of different natural isoforms. Eur. J. Biochem. 260 (1999) 421-429